Tetrahedron Letters p. 4983 - 4986 (1985)
Update date:2022-08-11
Topics:
Paquette, Leo A.
Ham, Won Hun
Dime, David S.
The tetracyclic epoxide 16 was prepared in stereocontrolled fashion from 4,4-dimethylcyclohexanone, the key steps being Saegusa ring expansion of its silyl enol ether to 5, ortho ester Claisen rearrangement of 7, and cyclization of 9 without rupture of th
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Doi:10.1016/S0040-4039(00)89235-7
(1985)Doi:10.1021/acs.inorgchem.8b02752
(2019)Doi:10.1021/jp002515i
(2001)Doi:10.1371/journal.pone.0107182
(2014)Doi:10.1080/00397919808004300
(1998)Doi:10.1021/ja01292a007
(1936)